DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM— 510(k) K080004
Substantially EquivalentSicel Technologies, Inc.
FDA 510(k) clearance K080004 for DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM, Substantially Equivalent on 2008-01-23. Applicant: Sicel Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Sicel Technologies, Inc.
- Product code
- Code NZT
- Device class
- Class 2
- Regulation
- 21 CFR 892.5050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Morrisville, NC, US
Recent devices under product code NZT
view allMore clearances from Sicel Technologies, Inc.
view all- K083035 — DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM
- K081859 — MODIFICATION TO ONEDOSE PATIENT DOSIMETRY SYSTEM
- K071399 — DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM, MODEL DVS-I-11: DVS INSERTION TOOL, DVS-D-A: DVS DOSIMETER, DVS-R-100
- K061051 — DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM, MODELS DVS-I-11, DVS INSERTION TOOL, DVS-D-A, DVS DOSIMETER
- K052118 — DOSE VERIFICATION SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.